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FDA Inspection 833696 — NuTech Spine, Inc.

NuTech Spine, Inc. — FEI 3009169996

The FDA completed an inspection of NuTech Spine, Inc. on April 30, 2013 in Birmingham, AL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 30, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Birmingham, AL (United States)

Facility

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FDA data resources